ClinGen Allele Registry
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Canonical Allele Identifier:
PA179976
Gene: DNAH11
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
177249
ClinVar RCV:
RCV000153157
RCV000271550
ClinVar Variation:
167000
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001264044.1:p.Ala3659Val
CA179975
NM_001277115.2:c.10976C>T